Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss (2011)
- Authors:
- Guerra-Shinohara, Elvira Maria
- Lázaro, Robson José
- Giusti, Kelma Cordeiro da Silva
- Britto, Jessica Carrilho
- Cavalcante, Silvana Henrique
- Boacnin, Marina do Rosário
- Gomes, Guilherme Wataru
- Carvalho, Mário Henrique Burlacchini de
- Amorim Filho, Antônio Gomes
- Zugaib, Marcelo
- D'Almeida, Vânia - Universidade Federal de São Paulo (UNIFESP)
- Guerra-Shinohara, Elvira Maria
- USP affiliated authors: SHINOHARA, ELVIRA MARIA GUERRA - FCF ; ZUGAIB, MARCELO - FM
- Unidades: FCF; FM
- Subjects: POLIMORFISMO; ABORTO ESPONTÂNEO
- Language: Inglês
- Imprenta:
- Publisher: Escola Superior de Tecnologia da Saúde
- Publisher place: Lisboa
- Date published: 2011
- Source:
- Título do periódico: Abstract Book
- Conference titles: International Conference on Homocysteine Metabolism
-
ABNT
GUERRA-SHINOHARA, Elvira Maria et al. Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. 2011, Anais.. Lisboa: Escola Superior de Tecnologia da Saúde, 2011. . Acesso em: 18 abr. 2024. -
APA
Guerra-Shinohara, E. M., Lázaro, R. J., Giusti, K. C. da S., Britto, J. C., Cavalcante, S. H., Boacnin, M. do R., et al. (2011). Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. In Abstract Book. Lisboa: Escola Superior de Tecnologia da Saúde. -
NLM
Guerra-Shinohara EM, Lázaro RJ, Giusti KC da S, Britto JC, Cavalcante SH, Boacnin M do R, Gomes GW, Carvalho MHB de, Amorim Filho AG, Zugaib M, D'Almeida V. Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. Abstract Book. 2011 ;[citado 2024 abr. 18 ] -
Vancouver
Guerra-Shinohara EM, Lázaro RJ, Giusti KC da S, Britto JC, Cavalcante SH, Boacnin M do R, Gomes GW, Carvalho MHB de, Amorim Filho AG, Zugaib M, D'Almeida V. Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. Abstract Book. 2011 ;[citado 2024 abr. 18 ] - Efeito de polimorfismos genéticos relacionados ao metabolismo de folato e da homocisteína na etiologia dos abortos espontâneos recorrentes
- Polymorphisms in fibrinogen (C.148C>T and C.455G>A) gene and thrombomodulin (C.1418C>T) gene and their role in the occurrence of recurrent miscarriages
- MTHFR gene polymorphisms are not associated with hematologic alterations in women with recurrent pregnancy losses
- Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss
- Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss
- Association between polymorphisms in the transcobalamin II gene (TC2 C. 776C> G and C. TC267C>G) and methylenetetrahydrofolate reductase gene (MTHFR 677C>T) and risk of having recurrent miscarriages
- Frequencies of autoantibodies in women with recurrent pregnancy losses
- The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss
- Polymorphisms in thrombin-activatable fibrinolysis inhibitor and plasminogen activator inhibitor type 1 in women with primary recurrent pregnancy loss
- Association between the polymorphisms MTHFR c. 677C>T and MTHFR c. 1298A>C and haplotypes with recurrent miscarriages
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